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Ullrich congenital muscular dystrophy 2

Disease Summary
Associated Targets (1)
Tbio

1


Mondo Description Any Ullrich congenital muscular dystrophy in which the cause of the disease is a mutation in the COL12A1 gene.
Uniprot Description A form of Ullrich muscular dystrophy, a congenital myopathy characterized by muscle weakness and multiple joint contractures, generally noted at birth or early infancy. The clinical course is more severe than in Bethlem myopathy.
Mondo Term and Equivalent IDs
MONDO:0014654:  Ullrich congenital muscular dystrophy 2
UMLS:C4225314: